A putative Drosophila homolog of the Huntington’s disease gene

By Li Zhen   Karlovich Chris A.   Fish Matthew P.   Scott Matthew P.   Myers Richard M.  

Human Molecular Genetics, Vol. 8, Iss. 9, 1999-09 ,pp. : 1807-1815

Oxford University Press

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Huntingtin’s WW domain partners in Huntington’s disease post-mortem brain fulfill genetic criteria for direct involvement in Huntington’s disease pathogenesis

By Passani Lucius A.   Bedford MarkT.  

Human Molecular Genetics, Vol. 9, Iss. 14, 2000-09 ,pp. : 2175-2182

Oxford University Press

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Decreased expression of striatal signaling genes in a mouse model of Huntington’s disease

By Luthi-Carter Ruth   Strand Andrew   Peters Nikki L.   Solano Steven M.   Hollingsworth Zane R.   Menon Anil S.   Frey Ariel S.   Spektor Boris S.   Penney Ellen B.   Schilling Gabriele   Ross Christopher A.   Borchelt David R.   Tapscott Stephen J.   Young Anne B.   Cha Jang-Ho J.   Olson James M.  

Human Molecular Genetics, Vol. 9, Iss. 9, 2000-05 ,pp. : 1259-1271

Oxford University Press

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Neurological abnormalities in a knock-in mouse model of Huntington’s disease

By Detloff P.J.  

Human Molecular Genetics, Vol. 10, Iss. 2, 2001-01 ,pp. : 137-144

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Inactivation of Drosophila Apaf-1 related killer suppresses formation of polyglutamine aggregates and blocks polyglutamine pathogenesis

By Sang Tzu-Kang  

Human Molecular Genetics, Vol. 14, Iss. 3, 2005-02 ,pp. : 357-372

Oxford University Press

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